ziprasidone hydrochloride

Product NDC
50090-3748
11-digit product format
500903748
Labeler code
50090
Product ID
50090-3748_e4731bb3-689f-461a-a72e-adfff1bdcf47
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ziprasidone HCl
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077561
Marketing category
ANDA
Marketing start
2012-05-14
Marketing end
0000-00-00
Substance
ZIPRASIDONE HYDROCHLORIDE
Active strength
20 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
defe29d6-6a09-c3aa-4400-b1130380ccc3Product name520231206

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-3748-0ziprasidone hydrochloride40 in 1 BOTTLECAPSULE404

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-3748ZIPRASIDONE HYDROCHLORIDE (ZIPRASIDONE HCL) CAPSULE [A-S MEDICATION SOLUTIONS]4Legacy NDC, 1 package rows20200122_cf8b2f6c-e36d-4f03-896c-b5b862f25ae3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
314286ziprasidone HCl 20 MG Oral CapsulePSNcf8b2f6c-e36d-4f03-896c-b5b862f25ae34
314286ziprasidone 20 MG Oral CapsuleSCDcf8b2f6c-e36d-4f03-896c-b5b862f25ae34
314286ziprasidone (as ziprasidone HCl monohydrate) 20 MG Oral CapsuleSYcf8b2f6c-e36d-4f03-896c-b5b862f25ae34

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-3748-05009037480040 CAPSULE in 1 BOTTLE (50090-3748-0) 40 capsule2018-10-300000-00-00NoNoCurrent